Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C4225200
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29 		0.500 Biomarker CTD_human

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C4225200
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29 		0.500 Biomarker GENOMICS_ENGLAND

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0013363
Disease: Dysautonomia
Dysautonomia 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0013421
Disease: Dystonia
Dystonia 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0025958
Disease: Microcephaly
Microcephaly 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0027746
Disease: Nerve Degeneration
Nerve Degeneration 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0029132
Disease: Disorder of the optic nerve
Disorder of the optic nerve 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0036572
Disease: Seizures
Seizures 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0563243
Disease: Poor coordination
Poor coordination 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C0852413
Disease: Abnormal muscle tone
Abnormal muscle tone 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C1806780
Disease: Increased CSF protein
Increased CSF protein 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C1833431
Disease: Subependymal cysts
Subependymal cysts 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C1836923
Disease: Gastrointestinal dysmotility
Gastrointestinal dysmotility 		0.100 Biomarker HPO

Entrez Id: 25828
Gene Symbol: TXN2
TXN2
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		0.100 Biomarker HPO